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Clinical Features of Genetically Proved Leber Hereditary Optic Neuropathy in China
Neuro-Ophthalmology, 09/26/08

Wang W et al. - clinical features of genetically proved LHON patients in china were documented. LHON patients in China shared similar clinical features with those reported in Western countries and other Asian countries. G11778A mutation accounted for nearly 90% LHON patients. T14484C and G3460A mutation patients showed better visual acuity recovery than 11778 mutation patients did. Some patients with G11778A mutation were associated with “MS-like” changes.

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Leber congenital amaurosis: Clinical correlations with genotypes, gene therapy trials update, and future directions
Journal of American Association for Pediatric Ophthalmology and Strabismus , 12/17/09

Molecular Screening of Rhodopsin and Peripherin/RDS Genes in Mexican Families with Autosomal Dominant Retinitis Pigmentosa
Current Eye Research, 12/17/09

Human Lipocalin-1 Association with 3H-Testosterone and 3H-Estradiol
Current Eye Research, 12/17/09

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Today in Neuro-Ophthalmology...keeping you current

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Precaruncular approach for medial orbital wall periosteal anchoring of the globe in oculomotor nerve palsy
Journal of American Association for Pediatric Ophthalmology and Strabismus , 12/17/09

Frequency of the superior rectus muscle overaction/contracture syndrome in unilateral fourth nerve palsy
Journal of American Association for Pediatric Ophthalmology and Strabismus , 12/17/09

Spectral domain optical coherence tomography for detection of foveal morphology in patients with nystagmus
Journal of American Association for Pediatric Ophthalmology and Strabismus , 12/17/09

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